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Synthesis of Ledipasvir through a Late-Stage Cyclopropanation and Fluorination Process
Synthesis ( IF 2.2 ) Pub Date : 2023-04-13 , DOI: 10.1055/s-0042-1751437 Gangarajula Sudhakar 1, 2 , Chennam Ramu 1, 2 , T. Kumaraguru 1, 2 , M. Sridhar Reddy 1, 2 , Haridas B. Rode 1, 2 , Subhash Ghosh 1, 2 , Ch. Raji Reddy 1, 2
中文翻译:
通过后期环丙烷化和氟化工艺合成 Ledipasvir
更新日期:2023-04-14
Synthesis ( IF 2.2 ) Pub Date : 2023-04-13 , DOI: 10.1055/s-0042-1751437 Gangarajula Sudhakar 1, 2 , Chennam Ramu 1, 2 , T. Kumaraguru 1, 2 , M. Sridhar Reddy 1, 2 , Haridas B. Rode 1, 2 , Subhash Ghosh 1, 2 , Ch. Raji Reddy 1, 2
Affiliation
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We have designed and developed an easily accessible advanced intermediate of ledipasvir that allowed late-stage cyclopropanation and difluorination, thereby providing a novel and more efficient process for the preparation of ledipasvir in the longest linear sequence of 8 steps with 20% overall yield.
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
通过后期环丙烷化和氟化工艺合成 Ledipasvir
我们设计并开发了一种易于获取的 ledipasvir 高级中间体,允许后期环丙烷化和二氟化,从而为以 20% 的总收率最长的 8 个步骤线性序列制备 ledipasvir 提供了一种新颖且更有效的工艺。